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Synthesis of pyrroloquinoline quinone in vivo and in vitro and detection of an intermediate in the biosynthetic pathway.

机译:体内和体外吡咯并喹啉醌的合成以及生物合成途径中中间体的检测。

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摘要

In Klebsiella pneumoniae, six genes, constituting the pqqABCDEF operon, which are required for the synthesis of the cofactor pyrroloquinoline quinone (PQQ) have been identified. The role of each of these K. pneumoniae Pqq proteins was examined by expression of the cloned pqq genes in Escherichia coli, which cannot synthesize PQQ. All six pqq genes were required for PQQ biosynthesis and excretion into the medium in sufficient amounts to allow growth of E. coli on glucose via the PQQ-dependent glucose dehydrogenase. Mutants lacking the PqqB or PqqF protein synthesized small amounts of PQQ, however. PQQ synthesis was also studied in cell extracts. Extracts made from cells containing all Pqq proteins contained PQQ. Lack of each of the Pqq proteins except PqqB resulted in the absence of PQQ. Extracts lacking PqqB synthesized PQQ slowly. Complementation studies with extracts containing different Pqq proteins showed that an extract lacking PqqC synthesized an intermediate which was also detected in the culture medium of pqqC mutants. It is proposed that PqqC catalyzes the last step in PQQ biosynthesis. Studies with cells lacking PqqB suggest that the same intermediate might be accumulated in these mutants. By using pqq-lacZ protein fusions, it was shown that the expression of the putative precursor of PQQ, the small PqqA polypeptide, was much higher than that of the other Pqq proteins. Synthesis of PQQ most likely requires molecular oxygen, since PQQ was not synthesized under anaerobic conditions, although the pqq genes were expressed.
机译:在肺炎克雷伯菌中,已鉴定出构成pqqABCDEF操纵子的六个基因,这些基因是辅因子吡咯并喹啉醌(PQQ)合成所必需的。通过克隆的pqq基因在不能合成PQQ的大肠杆菌中的表达来检查每种肺炎克雷伯菌Pqq蛋白的作用。所有六个pqq基因都是PQQ生物合成和排泄到培养基中所必需的,其数量足以允许E. coli通过PQQ依赖性葡萄糖脱氢酶在葡萄糖上生长。但是,缺少PqqB或PqqF蛋白的突变体合成了少量的PQQ。还对细胞提取物中的PQQ合成进行了研究。由含有所有Pqq蛋白的细胞制成的提取物含有PQQ。除PqqB之外的每种Pqq蛋白均缺乏,导致PQQ的缺失。缺乏PqqB的提取物会缓慢合成PQQ。用含有不同Pqq蛋白的提取物进行的补充研究表明,缺乏PqqC的提取物合成了一种中间体,该中间体也在pqqC突变体的培养基中检测到。建议PqqC催化PQQ生物合成的最后一步。对缺乏PqqB的细胞的研究表明,这些突变体中可能积累了相同的中间体。通过使用pqq-lacZ蛋白融合蛋白,表明PQQ的假定前体小PqqA多肽的表达远高于其他Pqq蛋白。 PQQ的合成很可能需要分子氧,因为尽管表达了pqq基因,但PQQ并不是在厌氧条件下合成的。

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